Metabolite Glucuronide form of tolfenamic acid
- Name
- Glucuronide form of tolfenamic acid
- Description
- Not Available
- Structure
- Synonyms
- Not Available
- UNII
- Not Available
- CAS number
- Not Available
- Weight
- Average: 409.82
Monoisotopic: 409.0928297 - Chemical Formula
- C19H20ClNO7
- InChI Key
- ORYXNFVXAIRHHF-UHFFFAOYSA-N
- InChI
- InChI=1S/C19H20ClNO7/c1-9-11(20)6-4-8-12(9)21-13-7-3-2-5-10(13)17(25)27-19-16(24)14(22)15(23)18(26)28-19/h2-8,14-16,18-19,21-24,26H,1H3
- IUPAC Name
- 3,4,5,6-tetrahydroxyoxan-2-yl 2-[(3-chloro-2-methylphenyl)amino]benzoate
- SMILES
- CC1=C(Cl)C=CC=C1NC1=CC=CC=C1C(=O)OC1OC(O)C(O)C(O)C1O
- Reactions
- Tolfenamic acid Glucuronide form of tolfenamic acid
- Spectra
- Chromatographic Properties
Collision Cross Sections (CCS)
Adduct CCS Value (Å2) Source type Source [M-H]- 180.7512 predictedDeepCCS 1.0 (2019) [M+H]+ 183.1092 predictedDeepCCS 1.0 (2019) [M+Na]+ 190.1022 predictedDeepCCS 1.0 (2019) - External Links
- Not Available
- Predicted Properties
Property Value Source Water Solubility 1.52 mg/mL ALOGPS logP 1.89 ALOGPS logP 3.69 Chemaxon logS -2.4 ALOGPS pKa (Strongest Acidic) 11.22 Chemaxon pKa (Strongest Basic) -2.2 Chemaxon Physiological Charge 0 Chemaxon Hydrogen Acceptor Count 7 Chemaxon Hydrogen Donor Count 5 Chemaxon Polar Surface Area 128.48 Å2 Chemaxon Rotatable Bond Count 5 Chemaxon Refractivity 99.14 m3·mol-1 Chemaxon Polarizability 40.15 Å3 Chemaxon Number of Rings 3 Chemaxon Bioavailability 1 Chemaxon Rule of Five Yes Chemaxon Ghose Filter Yes Chemaxon Veber's Rule No Chemaxon MDDR-like Rule No Chemaxon